CAP Hepatoblastoma Biopsy Cancer Protocol
Protocol for the Examination of Biopsy Specimens From Patients With HepatoblastomaVersion: Hepatoblastoma Biopsy 4.0.0.0Protocol Posting Date: February 2019Accreditation RequirementsThe use of this protocol is recommended for clinical care purposes but is not required for accreditation purposes. This protocol should be used for the following procedures AND tumor types:ProcedureDescriptionBiopsyIncludes specimens designated core biopsy, incisional biopsy, or otherTumor TypeDescriptionHepatoblastomaIncludes pediatric hepatoblastoma The following should NOT be reported using this protocol:ProcedureResection (consider Hepatoblastoma Resection protocol)Tumor TypeOther primary malignant hepatic tumorsAuthorsErin Rudzinski, MD*; Sarangarajan Ranganathan, MD*; John Hicks, MD; Grace Kim, MD With guidance from the CAP Cancer and CAP Pathology Electronic Reporting Committees* Denotes primary author. All other contributing authors are listed alphabetically.Important NoteFirst priority should be given to formalin-fixed tissues for morphologic evaluation. The second priority for tissue processing is snap-freezing up to 1 g (minimum of 100 mg) of tumor from grossly different regions for molecular studies, as well as viable sterile tumor for cytogenetic studies (see Explanatory Note A). Samples from the same foci should be collected for histology, with appropriate identification. Samples of nontumoral liver should be collected for snap-freezing as well.For more information, contact: The Children’s Oncology Group Biopathology Center; Phone: (614) 722-2890 or (800) 347-2486.Summary of Changesv4.0.0.0 - Biopsy and resection procedures separated into individual protocolsSurgical Pathology Cancer Case SummaryProtocol posting date: February 2019HEPATOBLASTOMA: BiopsyNote: This case summary is recommended for reporting Hepatoblastoma but is NOT REQUIRED for accreditation purposes. Core data elements are bolded to help identify routinely reported elements.Select a single response unless otherwise indicated.Procedure (Note A)___ Core biopsy___ Incisional biopsy___ Other (specify): _______________________________ Not specifiedTumor Site___ Right lobe___ Left lobe___ Right and left lobes___ Other (specify): _______________________________ Not specifiedTumor Focality (within liver)___ Unifocal___ Multifocal___ Cannot be determined (explain): _______________________________Histologic Type (select all that apply) (Note B) ___ Hepatoblastoma, epithelial type, fetal pattern (mitotically inactive) ___ Hepatoblastoma, epithelial type, fetal pattern (mitotically active) ___ Hepatoblastoma, epithelial type, embryonal___ Hepatoblastoma, epithelial type, pleomorphic (poorly differentiated) ___ Hepatoblastoma, epithelial type, macrotrabecular pattern ___ Hepatoblastoma, epithelial type, small cell undifferentiated pattern Percentage of tumor with this histologic feature (if possible): _____% ___ Hepatoblastoma, mesenchymal type without teratoid features ___ Hepatoblastoma, mesenchymal type with teratoid features ___ Hepatoblastoma, other (specify subtypes if not included): ________________________ Hepatocellular neoplasm, not otherwise specifiedNote: Ancillary studies (immunohistochemistry) may be performed to clarify histologic type.Additional Pathologic Findings (select all that apply) (Note C)___ No background liver available for evaluation (explain): ____________________________ None identified___ Cirrhosis/fibrosis (specify stage of fibrosis): __________ Iron overload___ Hepatitis (specify type): _______________________________ Other (specify): ____________________________Serum Alpha Fetoprotein (FP) Level (Note D) _____________Note: Level at time of diagnosis may be prognostically important.___ less than 100 ng/mL ___ 100 ng/mL – 1.2 million ng/mL___ greater than 1.2 million ng/ml___ Not known Ancillary Studies (select all that apply) (Note E) ___ INI1 immunohistochemistry performed ___ INI1 expression retained ___ INI1 expression lost ___ Glypican-3 immunohistochemistry performed ___ Negative ___ Positive___ Pattern of staining (specify): ___________ ___ Beta-catenin immunohistochemistry performed___ Negative (nuclear)___ Positive (nuclear)___ Other (specify): ______________________________Comment(s)Explanatory NotesA. ProceduresFine-Needle AspirationPrimary diagnosis by cytology (fine-needle aspiration) is not recommended as it may be misleading because of difficulties in distinguishing well-differentiated hepatocellular malignancy from regenerative changes and benign proliferations, and because of the variability of histologic features in hepatoblastoma. Hence, all attempts for fine-needle aspiration should be discouraged in favor of biopsy or resection.BiopsyThe current recommendation for diagnosis of hepatoblastoma is a biopsy if upfront resection is not an option. This is the recommendation made in a recent consensus classification paper and will be followed in all future Children’s Oncology Group (COG) and other international protocols for uniformity.PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Mb3Blei1UZXJyYWRhPC9BdXRob3I+PFllYXI+MjAxNDwv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ADDIN EN.CITE PEVuZE5vdGU+PENpdGU+PEF1dGhvcj5Mb3Blei1UZXJyYWRhPC9BdXRob3I+PFllYXI+MjAxNDwv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ADDIN EN.CITE.DATA 1 Hepatoblastomas are usually solitary lesions that occupy 1 or the other lobes of the liver, or may transgress more than 1 liver segment (the basis for pretreatment extent of disease [PRETEXT] staging). Multifocal lesions also occur, and multifocal tumors are the most likely cases to be diagnosed by biopsy. However, any tumor that is radiologically PRETEXT I or II or does not fit into stage I or II by the traditional COG staging system may be biopsied upfront, as primary resection may not be an option. Even with lower stage disease, large vessel invasion will be a contraindication to primary resection and will warrant preoperative chemotherapy. The type of biopsy performed is entirely up to the discretion of the treating physicians and surgeons. Biopsy types include image guided needle biopsy (the more common scenario in the US) or open biopsy for cases that are difficult to access or in which there is potential for surgical resection. While it is much easier to get adequate tissue for studies with open biopsies, a needle biopsy done in interventional radiology is adequate as long as multiple (5-10) needle cores are obtained.1 It is also recommended that the radiologist obtain needle cores from different portions of the tumor to maximize sampling of all areas of interest in the tumor. Calcified, bony, or hard tissue need not be sampled, however, and focus should be placed on obtaining adequate representation of the viable epithelial component. The region from which the biopsy is obtained should be noted if possible. If tumor involves more than 1 lobe, more than 1 lesion or area of the tumor should be sampled. These sites should be labeled separately, as different nodules in the same patient may have different histologies and biology. As most needle biopsy procedures are ultrasound guided, it may be easy to differentiate between tumor and uninvolved liver, and an attempt should be made to acquire adjacent nontumor liver tissue to understand underlying disease processes. Upfront biopsy necessitates proper triage of the specimen for all pathologic and biologic studies, as required for COG trials of most pediatric tumors. The goal of the biopsy is tissue diagnosis to separate hepatoblastomas (the most common pediatric tumors) from other benign (especially mesenchymal hamartoma, adenomas, and focal nodular hyperplasia) or malignant (pediatric hepatocellular carcinoma and embryonal sarcoma) liver tumors, therapy for which are different. Regardless of the procedure type, every attempt should be made intraoperatively to assess if tissue obtained is viable and can be triaged for other studies. Imprint cytology may be used to assess tumor viability. No tissue diagnosis is needed at the time of frozen section, for that is the purpose of doing the biopsy, and the surgeon should be so educated. Tissue should instead be set aside for snap freezing (tumor and normal) as well as for cytogenetics (tumor only). While tissue may be set aside for electron microscopy, it is left to individual Institutions to make that decision. For further details, pathologists are referred to the consensus classification of hepatoblastoma published by Lopez-Terrada et al.2References:1. Finegold MJ. Hepatic Tumors in Childhood. In: Russo P RE, Piccoli D, eds. Pathology of Pediatric Gastrointestinal and Liver Disease. New York, NY: Springer-Verlag; 2004:300-346.2. Lopez-Terrada D, Alaggio R, de Davila MT, et al. Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium. Mod Pathol. 2014;27(3):472-491.B. Histologic TypePrimary malignant tumors of the liver account for approximately 1% of all childhood cancer. The most common type is hepatoblastoma, which has an annual incidence of 0.9 per 1 million children.1 Not only are hepatoblastomas rare, but their diversity significantly limits the experience of any single center or pathologist. A classification scheme for hepatoblastoma that divides the more frequently or prognostically influential features from infrequent or inconsequential (minor) components is presented in Table 1.2 The significance of a biopsy classification is that it reflects the true components of the tumor and is not limited by chemotherapy effects that alter the morphology of these tumors. It should, however, be noted that not all components may necessarily be sampled in a biopsy, and radiologic features, especially the presence of bone, need to be considered for subtyping.Table 1. Pediatric Liver Tumors Consensus Classification Epithelial Tumors - HepatocellularBenign and tumor-like conditionsHepatocellular adenoma (adenomatosis)Focal nodular hyperplasiaMacroregenerative NodulePremalignant lesionsDysplastic nodulesMalignant HepatoblastomaEpithelial variantsPure fetal with low mitotic activityFetal, mitotically activePleomorphic, poorly differentiatedEmbryonalSmall-cell undifferentiatedINI1-negativeINI1-positiveEpithelial mixed (any/all above)CholangioblasticEpithelial macrotrabecular patternMixed epithelial and mesenchymalWithout teratoid featuresWith teratoid featuresHepatocellular carcinoma (HCC)Classic HCCFibrolamellar HCCHepatocellular neoplasm, not otherwise specified (NOS)Modified from Lopez-Terrada et al.2There is no relationship between the age of the child and the predominant cell type in hepatoblastoma.1,3 Of all cases at all ages, 85%-90% contain both fetal and embryonal derivatives in variable proportions; 20% have stromal derivatives. Because these histologic types tend to be randomly intermingled, both fine-needle aspiration and biopsies may capture a nonrepresentative sample of tumor. The most significant component to identify in a biopsy of a low-stage tumor is well-differentiated fetal histology characterized by uniform-appearing round to polygonal cells with small central nuclei and clear or pale eosinophilic cytoplasm that may give the tumor a light-cell dark-cell pattern.1,2 Nucleoli are usually inconspicuous and the mitotic rate is low (less than 2 mitoses per 10 high-power fields), the main criteria for this subtype. If the entire biopsy is composed only of this pattern, the possibility of primary resection should be advocated to minimize the need for chemotherapy if indeed the resected tumor appears histologically uniform. Again, this is only the case with low stage disease; higher stage diseases are likely to have other histologic components that are unsampled. It is important to realize that diagnosis of pure, well-differentiated fetal histology is to be made only on a completely resected tumor where adequate sampling excludes other areas and chemotherapy does not influence the morphology. The current Children’s Oncology Group (COG) study is treating stage I well-differentiated fetal hepatoblastoma (with low mitotic rate) with surgery alone.2-5 Distinguishing well-differentiated (mitotically inactive) fetal hepatoblastoma tumor cells from normal liver in an infant can be difficult. The fetal tumor cells are larger than normal fetal hepatocytes and have a higher nuclear-to-cytoplasmic ratio. The nuclei are regular and round with little discernible mitotic activity (less than 2 mitoses per 10 high-power [X40 objective] fields) in the well-differentiated variety.2,5 Fetal tumor cells grow in cords, as in normal liver, or in nests or nodules. Clusters of normoblasts (extramedullary hematopoiesis) are seen, as in fetal liver. The cytoplasm of the fetal tumor cells varies from eosinophilic to clear, depending on the amount of glycogen content. Fetal tumor cells may also contain abundant lipid, producing vacuolization. In well-differentiated fetal tumors, bile secretion may be observed. Histologically, the mitotically active fetal pattern shows greater than or equal to 2 mitoses per 10 high-power fields. Cells are arranged in trabeculae with abundant eosinophilic granular cytoplasm and round centrally placed nuclei with indistinct to occasional conspicuous nucleoli. Extramedullary hematopoiesis is frequently encountered in these areas. The embryonal pattern is composed of cells with high nuclear-to-cytoplasmic ratio with oval to angulated nuclei that are hyperchromatic with prominent single nucleoli and scant cytoplasm. Rosettes and tubular structures may be seen in this component. Purely embryonal tumors are almost never encountered and invariably show some fetal areas.When tumor cells of either fetal or embryonal type show prominent nucleoli and more atypical morphology resembling hepatocellular carcinoma, the term pleomorphic epithelial is used. Most instances of these pleomorphic (also previously called anaplastic fetal) epithelial components are seen post resection, but one should be aware of this possibility in a biopsy. Arrangement of cells with fetal or embryonal morphology in areas in a trabecular arrangement where trabeculae are greater than 5 cells thick would warrant a description of macrotrabecular arrangement. This modification of cell thickness for plates was introduced in the new consensus classification, as the original 20-cell-thick plates were unusual and may represent hepatocellular carcinomas in a proportion of cases. The other significant epithelial component that needs to be looked for is the small cell undifferentiated (SCU) pattern.6 This is especially true if the entire biopsy or a significant portion of the biopsy shows this morphology. The more common scenario, however, is an epithelial hepatoblastoma with fetal and embryonal areas showing focal aggregates of small cells. These cells have uniform pale nuclei as compared to surrounding darker staining embryonal cells and are arranged in indistinct nests, which can be easily missed on histology. Immunohistochemistry may aid in this diagnosis, and care should be taken to differentiate a predominant SCU pattern from malignant rhabdoid tumor (MRT). Rhabdoid tumor cells have the characteristic, eccentric, pink cytoplasmic inclusions (periodic acid-Schiff/diastase positive, vimentin or cytokeratin positive) with vesicular nuclei and fibrillar inclusion bodies by electron microscopy. They may be associated with the small cell component in otherwise typical hepatoblastomas or as the exclusive cell type, in which case they occur in infancy and are associated with a poor prognosis. The classic rhabdoid tumors show loss of INI1 staining due to INI1 gene mutation and are treated on the MRT protocol (see Note E).When first distinguished from embryonal epithelium, small undifferentiated cells in hepatoblastoma were noted to resemble neuroblastoma, to have a low mitotic rate, and were called anaplastic, consistent with the dictionary definition, characterized by imperfect development. Because anaplastic was redefined by Faria et al7 for Wilms tumor as nuclear enlargement to 3 times that of typical tumor cells, hyperchromasia, and atypical mitoses, the small cell undifferentiated component is no longer designated as anaplastic. Beckwith-type anaplasia does occur rarely in hepatoblastoma, and its significance is unknown. The small cells have been considered putative hepatic progenitor cells on the basis of immunohistochemical and electron microscopic studies. When present in a significant fraction of the hepatoblastoma (75%) or as the sole cell type, the small cell type is typically found in infants younger than 1 year; they have a poor prognosis, with poor response to current therapy. The prognostic significance of smaller proportions of the small cell undifferentiated type is still undetermined. The majority of tumors will show a mixed pattern of components, either epithelial alone or epithelial admixed with mesenchymal and even teratoid components. Even if mesenchymal components are not visualized histologically in a biopsy, radiologic documentation of bone or calcification may reflect a mixed epithelial-mesenchymal hepatoblastoma and help in the differential from other tumors. In some instances, biopsies may reveal primitive spindled cells at the edges of nodules of hepatoblastoma, mimicking small cells, but outside of nodules. These areas represent primitive mesenchyme, sometimes called “blastema” due to their ability to differentiate into epithelial or mesenchymal elements.Often, mixed hepatoblastomas contain epithelial membrane antigen (EMA)-positive nests of squamous epithelium. The osteoid component of mixed hepatoblastomas is found to be a matrix of collagen surrounding cells expressing EMA and having ultrastructural features of epithelium, rather than osteoblasts. Hepatoblastomas may contain other stromal derivatives, including cartilage and rhabdomyoblasts. There is no prognostic significance to the presence of mixed histologic features.Other unusual components that may be seen on a biopsy include the cholangioblastic pattern, neuroepithelium, glandular component (intestinal type), and even squamous elements.2,8 Retinal pigment or immature neuroepithelial rosettes warrant a diagnosis of teratoid hepatoblastoma. These are usually intermingled with more classic morphology of hepatoblastomas. Teratoid hepatoblastoma was initially depicted as having intestinal, neural, and melanocytic elements. These are distinguished from true teratomas, which can also occur in the livers of children, on the basis of organoid differentiation and even greater diversity of tissue elements in the teratomas. Multinucleated tumor giant cells are found in rare hepatoblastomas, sometimes associated with human chorionic gonadotropin (HCG) production and clinical virilization. References:1. Finegold MJ. Hepatic Tumors in Childhood. In: Russo P RE, Piccoli D, eds. Pathology of Pediatric Gastrointestinal and Liver Disease. New York, NY: Springer-Verlag; 2004:300-346.2. Lopez-Terrada D, Alaggio R, de Davila MT, et al. Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium. Mod Pathol. 2014;27(3):472-491.3. Czauderna P, Lopez-Terrada D, Hiyama E, H?berle B, Malogolowkin MH, Meyers RL. Hepatoblastoma state of the art: pathology, genetics, risk stratification, and chemotherapy. Curr Opin Pediatr. 2014;26(1):19-28. 4. Meyers RL, Tiao G, de Ville de Goyet J, Superina R, Aronson DC. Hepatoblastoma state of the art: pre-treatment extent of disease, surgical resection guidelines and the role of liver transplantation. Curr Opin Pediatr. 2014;26(1):29-36.5. Malogolowkin MH, Katzenstein HM, Meyers RL, et al. Complete surgical resection is curative for children with hepatoblastoma with pure fetal histology: a report from the Children's Oncology Group. J Clin Oncol. 2011;29(24):3301-3306.6. Trobaugh-Lotrario AD, Tomlinson GE, Finegold MJ, Gore L, Feusner JH. Small cell undifferentiated variant of hepatoblastoma: adverse clinical and molecular features similar to rhabdoid tumors. Pediatr Blood Cancer. 2009;52(3):328-334. 7. Faria P, Beckwith JB, Mishra K, et al. Focal versus diffuse anaplasia in Wilms tumor--new definitions with prognostic significance: a report from the National Wilms Tumor Study Group. Am J Surg Pathol. 1996;20(8):909-920. Review.8.Rudzinski ER, Bahrami A, Parham DM, Sebire N. Protocol for the Examination of Specimens from Pediatric Patients with Rhabdomyosarcoma (Version 3.2.0.2) College of American Pathologists, August 2016; (accessed 8/1/2018; available at cancerprotocols).C. Associated Clinical, Environmental, and Genetic FactorsClinical Features and Differential DiagnosisThe presenting symptom of virtually all liver tumors in children is abdominal swelling secondary to hepatomegaly. When confronted with this symptom, it is useful to consider the age at which liver tumors tend to occur (see Table 2).1 Exceptions are frequent, but age can serve as a guide when the presenting symptoms lack specificity. In the Pediatric Oncology Group series from 1986 to 2002,2,3 66% of hepatoblastomas were manifest by the second year, and 11% before 6 months of age. Approximately 50% of those in infants were congenital, given their size when discovered by 2-3 months of age; 6% of hepatoblastomas occurred after 5 years of age. Hepatocellular carcinomas have been observed as early as 6 months of age. Seven examples of mixed hepatoblastomas and hepatocellular carcinomas have been observed at a mean age of 8.5 years; perinatally acquired hepatitis B virus was responsible in 3 instances. Yolk sac tumors are more common in early childhood, but they also occur rarely in older adults. Systemic malignancies and metastatic disease must be considered at all ages because hepatomegaly due to megakaryoblastic leukemia, Langerhans cell histiocytosis, and neuroblastoma are important sources of confusion with hepatoblastoma in infancy, as are intraabdominal desmoplastic small round cell tumors later in childhood.Table 2. Tumors of the Liver in Children: Usual Age of PresentationAgeBenignMalignantInfancy(0-1 y)HemangioendotheliomaMesenchymal hamartomaTeratomaHepatoblastoma, especially small cell undifferentiatedRhabdoid tumorYolk sac tumorLangerhans cell histiocytosisMegakaryoblastic leukemiaDisseminated neuroblastomaEarly childhood(1-3 y)HemangioendotheliomaMesenchymal hamartomaHepatoblastomaRhabdomyosarcomaInflammatory myofibroblastic (pseudo) tumorLater childhood(3-10 y)Perivascular epithelioid cell tumors (PE-Comas), including angiomyolipoma in liver and clear cell tumor of ligamentum teres / falciform ligamentHepatocellular carcinomaEmbryonal (undifferentiated) sarcomaAngiosarcomaCholangiocarcinomaEndocrine (gastrin) carcinomaAdolescence(10-16 y)AdenomaFocal nodular hyperplasiaBiliary cystadenomaFibrolamellar hepatocellular carcinomaHodgkin lymphomaLeiomyosarcomaEnvironmental FactorsHepatoblastoma occurs in association with several well-described environmental factors and cancer genetic syndromes (see Table 3); however, not all of these associations are necessarily of statistical significance. Environmental factors and prenatal exposure to different agents have been implicated in hepatoblastoma.4,5Data from the US National Cancer Institute Surveillance, Epidemiology, and End Result (SEER) program revealed an average annual increase of 5.2% in the incidence of hepatoblastoma from 1973 to 1992.2 This change might be explained by hepatoblastoma occurring in surviving premature infants. Hepatoblastomas in Japan accounted for 58% of all malignancies in children who weighed less than 1000g at birth. Further analysis of the Japanese Children’s Cancer Registry data revealed that 15 of 303 (5%) hepatoblastomas between 1985-1995 occurred in infants with a history of prematurity and weight less than 1500g at birth.4 This rate was greater than 10 times that for all live births. The histologic features of hepatoblastoma after prematurity are indistinguishable from those of other hepatoblastomas.The Children’s Cancer Group has evaluated environmental or drug exposure. Seventy-five sets of parents of children with hepatoblastoma were compared with the parents of age-matched controls. In the group of children with hepatoblastoma, there was a significant excess of maternal exposure, before and during pregnancy, to metals used in welding and soldering, lubricating oils, and protective greases.6 Paternal exposure to metals was also greater. Table 3. Clinical Syndromes, Congenital Malformations, and Other Conditions Associated With HepatoblastomaCongenital MalformationsAbsence of left adrenal glandBilateral talipesDuplicated uretersDysplasia of ear lobesCleft palateFetal hydropsHemihypertrophyHeterotopic lung tissueHorseshoe kidneyInguinal herniaIntrathoracic kidneyMacroglossia Meckel diverticulumPersistent ductus arteriosusRenal dysplasiaRight-sided diaphragmatic herniaSingle coronary arteryUmbilical herniaSyndromesBeckwith-Wiedemann syndromeBeckwith-Wiedemann syndrome with opsoclonus, myoclonusBudd-Chiari syndromeFamilial adenomatous polyposis syndromeLi-Fraumeni cancer syndromePolyposis coli familiesSchinzel-Geidion syndromeSimpson-Golabi-Behmel syndromeTrisomy 18Metabolic / Pathophysiologic AbnormalitiesCystathioninuriaGlycogen storage disease types Ia, III, and IVHypoglycemiaHeterozygous ?1-antitrypsin deficiencyIsosexual precocityPrematurityTotal parenteral nutritionVery low birth weightEnvironmental / OtherAlcohol embryopathyHuman immunodeficiency virus or hepatitis B virus infectionMaternal clomiphene citrate or PergonalOral contraceptive, motherOral contraceptive, patientOsteoporosisSynchronous Wilms tumorGenetic FactorsKaryotyping of hepatoblastomas has revealed a recurrent pattern of chromosomal abnormalities.7 The most common karyotypic changes are extra copies of entire chromosomes (trisomies), sometimes in conjunction with other complex structural changes and often in association with double-minute chromosomes. Trisomies of chromosomes 2 and 20 have each been reported most commonly, and each of these trisomies has been reported as a sole karyotypic event, suggesting that they may represent an early stage of tumor evolution. Trisomy of chromosome 20 and duplication of the long arm of chromosome 20 have also been observed in rhabdomyosarcoma, suggesting a link between these 2 embryonal tumors, both of which are also associated with losses at the Beckwith-Wiedemann syndrome locus.8 Trisomy of chromosome 8 is also common; other trisomies are seen with lesser frequency. Occasional losses of entire chromosomes are seen, and these, too, are not random. The clinical significance of trisomies is unknown at present, although a recent study using comparative genomic hybridization has suggested that chromosomal gains at chromosomes 8 and 20 may be associated with an adverse prognosis.9Numerous recent studies have documented molecular genetic abnormalities in hepatoblastomas (see Table 4) and other hepatic tumors. Several genetic changes are shared with other embryonal tumors, such as loss of heterozygosity at chromosome 11p15, also described in rhabdomyosarcomas and Wilms tumors. Acquired mutations of the APC gene and the beta-catenin gene, both members of the Wnt signaling pathway, have also been reported in hepatoblastoma.7-11 The high frequency of beta-catenin mutations in hepatoblastomas and the increased incidence of hepatoblastomas in familial adenomatous polyposis families suggest the important role of an overactivation of wingless/Wnt pathway in the pathogenesis of hepatoblastoma. Collection of fresh or frozen hepatoblastoma tumor material as well as nontumoral liver tissue from these patients will be of great importance to the further investigation of the clinical relevance of these and other molecular genetic abnormalities in predicting the prognosis and clinical behavior of these tumors.Table 4. Constitutional Genetic Disease Associated With HepatoblastomaDiseaseTumor TypeChromosomal LocusGeneFamilial adenomatous polyposisHepatoblastoma, hepatocellular carcinoma or adenoma, biliary adenoma5q21.22APCBeckwith-Wiedemann syndromeHepatoblastoma, hemangioendothelioma11p15.5p57KIP2, othersLi-Fraumeni syndromeHepatoblastoma, undifferentiated sarcoma17p13TP53Trisomy 18Hepatoblastoma18—Glycogen storage disease types Ia, III, IVHepatocellular adenoma or carcinoma, hepatoblastoma17Glucose-6-phosphatase; debrancher and brancher enzymesReferences:Malogolowkin MH, Katzenstein HM, Meyers RL, et al. Complete surgical resection is curative for children with hepatoblastoma with pure fetal histology: a report from the Children's Oncology Group. J Clin Oncol. 2011;29(24):3301-3306.Ross JA, Gurney JG. Hepatoblastoma incidence in the United States from 1973 to 1992. Med Pediatr Oncol. 1998;30(3):141-142.Ortega JA, Douglass EC, Feusner JH, et al. Randomized comparison of cisplatin/vincristine/fluorouracil and cisplatin/continuous infusion doxorubicin for treatment of pediatric hepatoblastoma: a report from the Children's Cancer Group and the Pediatric Oncology Group. J Clin Oncol. 2000;18(14):2665-2675.Ikeda H, Hachitanda Y, Tanimura M, Maruyama K, Koizumi T, Tsuchida Y. Development of unfavorable hepatoblastoma in children of very low birth weight: results of a surgical and pathologic review. Cancer. 1998;82(9):1789-1796.Spector LG, Birch J. The epidemiology of hepatoblastoma. Pediatr Blood Cancer. 2012;59(5):776-779.Buckley JD, Sather H, Ruccione K, et al. A case-control study of risk factors for hepatoblastoma: a report from the Children's Cancer Study Group. Cancer. 1989;64:1169-1176.Fletcher JA, Kozakewich HP, Pavelka K, et al. Consistent cytogenetic aberrations in hepatoblastoma: a common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies? Genes Chromosomes Cancer. 1991;3(1):37-43.Steenman M, Tomlinson G, Westerveld A, Mannens M. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma. Cytogenet Cell Genet. 1999;86:157-161.Weber RG, Pietsch T, von Schweinitz D, Lichter P. Characterization of genomic alterations in hepatoblastomas: a role for gains on chromosomes 8q and 20 as predictors of poor outcome. Am J Pathol. 2000;157:571-578.Trobaugh-Lotrario AD, Venkatramani R, Feusner JH. Hepatoblastoma in children with Beckwith-Wiedemann syndrome: does it warrant different treatment? J Pediatr Hematol Oncol. 2014;36(5):369-373.Jeng YM, Wu MZ, Mao TL, Chang MH, Hsu HC. Somatic mutations of beta-catenin play a crucial role in the tumorigenesis of sporadic hepatoblastoma. Cancer Lett. 2000;152(1):45-51.D. Tumor MarkersSerum -fetoprotein (FP) is the most useful indicator of hepatocellular neoplasia. Levels of serum FP are markedly elevated in 80%-90% of hepatoblastomas and in 60%-70% of hepatocellular carcinomas.1,2 Lesser degrees of elevation in infants can be due to variations in the rate of decline after birth or to secretion from regenerating hepatocytes adjacent to hemangioendotheliomas or mesenchymal hamartomas. Therefore, it is unacceptable practice to institute chemotherapy for mass lesions of the liver based solely on imaging studies and serum FP levels. FP also can be elevated in yolk sac tumors, which may occur as primary tumors in the liver or together with hepatoblastoma. On the contrary, FP levels will not be increased when hepatoblastomas are primarily composed of the small cell undifferentiated type or in most fibrolamellar carcinomas, but even some typical fetal hepatoblastomas have failed to produce detectable increases in serum FP levels. Low FP levels below 100 ng/dL are therefore considered to be a poor prognostic indicator based on a large retrospective review of Children’s Hepatic tumor International Collaboration (CHIC) database.2-5 Following the FP level in patients with unresectable hepatoblastoma after chemotherapy may have prognostic value.References:1. Finegold MJ. Hepatic Tumors in Childhood. In: Russo P RE, Piccoli D, eds. Pathology of Pediatric Gastrointestinal and Liver Disease. New York, NY: Springer-Verlag; 2004:300-346.2. Czauderna P, Lopez-Terrada D, Hiyama E, H?berle B, Malogolowkin MH, Meyers RL. Hepatoblastoma state of the art: pathology, genetics, risk stratification, and chemotherapy. Curr Opin Pediatr. 2014;26(1):19-28.3.Lopez-Terrada D, Alaggio R, de Davila MT, et al. Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium. Mod Pathol. 2014;27(3):472-491.4.Meyers RL, Tiao G, de Ville de Goyet J, Superina R, Aronson DC. Hepatoblastoma state of the art: pre-treatment extent of disease, surgical resection guidelines and the role of liver transplantation. Curr Opin Pediatr. 2014;26(1):29-36.5.Meyers RL, Rowland JR, Krailo M, Chen Z, Katzenstein HM, Malogolowkin MH. Predictive power of pretreatment prognostic factors in children with hepatoblastoma: a report from the Children's Oncology Group. Pediatr Blood Cancer. 2009;53(6):1016-1022.E. Ancillary StudiesImmunohistochemistry may help differentiate hepatoblastoma from normal liver or other hepatocellular tumors, or aid in accurate diagnosis of the various hepatoblastoma subtypes. Staining with glypican-3 has a distinctive pattern with a fine pericanalicular staining seen in cells of the well-differentiated fetal hepatoblastoma, while the mitotically active fetal subtype and embryonal areas show similar patterns of coarse granular cytoplasmic staining. Small cell undifferentiated, cholangioblastic, and mesenchymal components are negative for glypican-3. Most teratoid components are also negative, except for an occasional glandular/yolk sac-like component that may show positive staining.Beta-catenin staining is more variable. Rare pediatric hepatocellular carcinomas can show strong positive staining, as can nested epithelial-stromal tumors. The tumor currently considered under the rubric of hepatocellular neoplasms, NOS in the consensus classification also show nuclear beta-catenin staining despite morphologic overlap with features of hepatocellular carcinomas. At present, there is no immunostain to differentiate hepatocellular carcinoma from hepatoblastoma with confidence, though in general most pediatric hepatocellular carcinomas do not show the same intense nuclear staining as hepatoblastomas. Beta-catenin staining is usually associated with strong glutamine synthetase and cyclin D1 staining in hepatoblastomas. Possible genetic markers (trisomies for chromosomes 2, 20, and 8; abnormalities of chromosome 1p) are being investigated and may help differentiate these 2 entities, but only approximately 35%-40% of hepatoblastomas carry the abnormalities.1Immunohistochemistry with glypican-3, beta-catenin, and glutamine synthetase (GS) aids in distinguishing hepatoblastoma from normal liver. Normal fetal liver is negative for glypican and shows only pericentral hepatocyte staining while staining diffusely in the tumor cells. Nuclear beta-catenin is only seen in tumor. Immunohistochemistry may be useful for identifying the small cell component of hepatoblastoma, as well. The small cells usually stain strongly and uniformly with beta-catenin in a nuclear pattern and are negative for glypican-3. This is in contrast to embryonal and fetal cells, which are cytoplasmic glypican-3 positive in most instances and show variable nuclear beta-catenin. The SCU component may also stain for vimentin and cytokeratin. Evaluation of the SCU component with an INI1 stain is critical, particularly if the SCU component forms a significant portion of the biopsy. Any loss of INI1 in the SCU component may warrant reclassification on review as a malignant rhabdoid tumor with a different Children’s Oncology Group treatment protocol. While this loss of INI1 is unusual in the usual SCU components that form small foci in between other epithelial components, it is prudent to do the stain and report the findings. Interestingly, stain for INI1 may be stronger in the nuclei of SCU component than surrounding cells; the significance of this is still to be determined. It is also important to realize that fetal pattern hepatoblastoma may resemble the fetal hepatocytes trapped in benign liver tumors, such as mesenchymal hamartoma (MH) and infantile hemangioma (IH), and this needs to be recognized in a biopsy. Use of immunohistochemistry may be helpful in some instances but usually needs more than 1 stain for confirmation. The fetal liver trapped in an MH or IH may show fine glypican-3 staining but will usually lack beta-catenin nuclear staining. Also, the lesional cells of IH will stain with CD31 and Glut1, while MH may show epithelial lined cysts or myxoid matrix with a prominent biliary component. The biliary elements in hepatoblastoma (Cholangioblastic pattern) usually show nuclear beta-catenin staining.References:1.Lopez-Terrada D, Alaggio R, de Davila MT, et al. Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium. Mod Pathol. 2014;27(3):472-491. ................
................
In order to avoid copyright disputes, this page is only a partial summary.
To fulfill the demand for quickly locating and searching documents.
It is intelligent file search solution for home and business.
Related download
Related searches
- inclusion body myositis biopsy findings
- muscle biopsy for myositis
- cpt laparoscopic biopsy peritoneal
- skin biopsy dermatomyositis
- when to biopsy thyroid nodules
- mri guided prostate biopsy procedure
- prostate biopsy preparation
- enema prostate biopsy best method
- mri guided prostate biopsy locations
- transperineal prostate biopsy enema
- prostate biopsy procedure
- ct biopsy adrenal cpt code